Canonical Allele Identifier: CA1335317523

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232542992C= , CM000664.2:g.232542992C=	GRCh38
NC_000002.11:g.233407702C= , CM000664.1:g.233407702C=	GRCh37
NC_000002.10:g.233115946C=	NCBI36
NG_012954.1:g.8266C=
NG_012954.2:g.8301C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000651502.1:c.715C= MANE Select	ENSP00000498757.1:p.Arg239=
ENST00000389492.3:c.559C=	ENSP00000374143.3:p.Arg187=
ENST00000389494.7:c.715C=	ENSP00000374145.3:p.Arg239=
NM_005199.4:c.715C=	NP_005190.4:p.Arg239=
NM_005199.5:c.715C= MANE Select	NP_005190.4:p.Arg239=